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Immunologically Inert Nanostructures as Selective Therapeutic Tools in Inflammatory Diseases

The current therapies based on immunosuppressant or new biologic drugs often show some limitations in term of efficacy and applicability, mainly because of their inadequate targeting and of unwanted adverse reactions they generate. To overcome these inherent problems, in the last decades, innovative...

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Detalles Bibliográficos
Autores principales: Talamini, Laura, Matsuura, Eiji, De Cola, Luisa, Muller, Sylviane
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8004653/
https://www.ncbi.nlm.nih.gov/pubmed/33806746
http://dx.doi.org/10.3390/cells10030707
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author Talamini, Laura
Matsuura, Eiji
De Cola, Luisa
Muller, Sylviane
author_facet Talamini, Laura
Matsuura, Eiji
De Cola, Luisa
Muller, Sylviane
author_sort Talamini, Laura
collection PubMed
description The current therapies based on immunosuppressant or new biologic drugs often show some limitations in term of efficacy and applicability, mainly because of their inadequate targeting and of unwanted adverse reactions they generate. To overcome these inherent problems, in the last decades, innovative nanocarriers have been developed to encapsulate active molecules and offer novel promising strategies to efficiently modulate the immune system. This review provides an overview of how it is possible, exploiting the favorable features of nanocarriers, especially with regard to their immunogenicity, to improve the bioavailability of novel drugs that selectively target immune cells in the context of autoimmune disorders and inflammatory diseases. A focus is made on nanoparticles that selectively target neutrophils in inflammatory pathologies.
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spelling pubmed-80046532021-03-29 Immunologically Inert Nanostructures as Selective Therapeutic Tools in Inflammatory Diseases Talamini, Laura Matsuura, Eiji De Cola, Luisa Muller, Sylviane Cells Review The current therapies based on immunosuppressant or new biologic drugs often show some limitations in term of efficacy and applicability, mainly because of their inadequate targeting and of unwanted adverse reactions they generate. To overcome these inherent problems, in the last decades, innovative nanocarriers have been developed to encapsulate active molecules and offer novel promising strategies to efficiently modulate the immune system. This review provides an overview of how it is possible, exploiting the favorable features of nanocarriers, especially with regard to their immunogenicity, to improve the bioavailability of novel drugs that selectively target immune cells in the context of autoimmune disorders and inflammatory diseases. A focus is made on nanoparticles that selectively target neutrophils in inflammatory pathologies. MDPI 2021-03-23 /pmc/articles/PMC8004653/ /pubmed/33806746 http://dx.doi.org/10.3390/cells10030707 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ).
spellingShingle Review
Talamini, Laura
Matsuura, Eiji
De Cola, Luisa
Muller, Sylviane
Immunologically Inert Nanostructures as Selective Therapeutic Tools in Inflammatory Diseases
title Immunologically Inert Nanostructures as Selective Therapeutic Tools in Inflammatory Diseases
title_full Immunologically Inert Nanostructures as Selective Therapeutic Tools in Inflammatory Diseases
title_fullStr Immunologically Inert Nanostructures as Selective Therapeutic Tools in Inflammatory Diseases
title_full_unstemmed Immunologically Inert Nanostructures as Selective Therapeutic Tools in Inflammatory Diseases
title_short Immunologically Inert Nanostructures as Selective Therapeutic Tools in Inflammatory Diseases
title_sort immunologically inert nanostructures as selective therapeutic tools in inflammatory diseases
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8004653/
https://www.ncbi.nlm.nih.gov/pubmed/33806746
http://dx.doi.org/10.3390/cells10030707
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